The paramagnetic NMR study of saddledmetalloporphyrins&;#61485;1. Characterization of Saddled Nickel(III)Porphyrin Cation Radical :The NMR ExplicativeModel for Ferromagnetically CoupledMetalloporphyrin Radical.2. Saddle-shaped six-coordinate iron(III) porphyrincomplex with unusual intermediate-spinelectronic structure

博士 === 中興大學 === 化學系所 === 102 === The two-electron oxidized NiII(OETPP)( 2,3,7,8,12,13,17,18-Octaethyl-5,10,15,20-tetraphenylporphyrin), which had merely been generated by eletrooxidation, is first chemically synthesized by addition of one equiv. of Br2 in benzene solution. The detailed magnetic prop...

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Main Authors: Chiao-Han Ting, 丁橋瀚
Other Authors: 陳炳宇
Format: Others
Language:zh-TW
Published: 2014
Online Access:http://ndltd.ncl.edu.tw/handle/78982289555784286133
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spelling ndltd-TW-102NCHU50650992015-12-10T04:01:53Z http://ndltd.ncl.edu.tw/handle/78982289555784286133 The paramagnetic NMR study of saddledmetalloporphyrins&;#61485;1. Characterization of Saddled Nickel(III)Porphyrin Cation Radical :The NMR ExplicativeModel for Ferromagnetically CoupledMetalloporphyrin Radical.2. Saddle-shaped six-coordinate iron(III) porphyrincomplex with unusual intermediate-spinelectronic structure 馬鞍型&;#63754;屬&;#21343;?順磁核磁共振光譜之研究 Chiao-Han Ting 丁橋瀚 博士 中興大學 化學系所 102 The two-electron oxidized NiII(OETPP)( 2,3,7,8,12,13,17,18-Octaethyl-5,10,15,20-tetraphenylporphyrin), which had merely been generated by eletrooxidation, is first chemically synthesized by addition of one equiv. of Br2 in benzene solution. The detailed magnetic properties are well characterized by EPR zero-field splitting (D), paramagnetic NMR analyses and DFT calculations to elucidate the electron configuration from two plausible states with similar spin distributions in ring macrocycle to be Ni(III) low-spin (dxy2dxz,yz4dz21dx2-y20, S =1/2) orthogonally coupled with a1u radical to form a triplet state. The spin state of iron(III) porphyrin complexes could be modulated by the axial ligand and the deformation of macrocycle ring. The 4-CNPy ligand, which acts as a weak base, has been reported to be the axial ligand in the [FeIII(OETPP)(4-CNPy)2]+ complex with pure intermediate-spin state (S = 3/2). However, the electronic configuration for this complex is controversial, there are four conjectures 4 in E the literatures, including 4 E (dxz,yz3dxy1dz21), 4 4 A1 (dxy2dxz,yz2dz21),(anti,dxy2dxz,yz2dz21dx2-y21a2u1) and A1 (anti,dxz,yz3 dxy1dz21dx2-y21a2u1). In our report, Density function theory (DFT) calculations combined with paramagnetic NMR analyses have shown the Fermi contact spin densities of 4E are more consistent with experimental data. Furthermore, through the decomposition energy composed of two fragments, containing iron porphyrin and axial cyanopyridines, the bonding interaction between iron-dxy&;#61472;and porphyrin-a1u orbitals stabilizes the intermediate spin electronic structure. Aside from the σ donating , the axial 4-CNPy also acts mainly as a π-donor instead of a π-acceptor. 陳炳宇 2014 學位論文 ; thesis 132 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 博士 === 中興大學 === 化學系所 === 102 === The two-electron oxidized NiII(OETPP)( 2,3,7,8,12,13,17,18-Octaethyl-5,10,15,20-tetraphenylporphyrin), which had merely been generated by eletrooxidation, is first chemically synthesized by addition of one equiv. of Br2 in benzene solution. The detailed magnetic properties are well characterized by EPR zero-field splitting (D), paramagnetic NMR analyses and DFT calculations to elucidate the electron configuration from two plausible states with similar spin distributions in ring macrocycle to be Ni(III) low-spin (dxy2dxz,yz4dz21dx2-y20, S =1/2) orthogonally coupled with a1u radical to form a triplet state. The spin state of iron(III) porphyrin complexes could be modulated by the axial ligand and the deformation of macrocycle ring. The 4-CNPy ligand, which acts as a weak base, has been reported to be the axial ligand in the [FeIII(OETPP)(4-CNPy)2]+ complex with pure intermediate-spin state (S = 3/2). However, the electronic configuration for this complex is controversial, there are four conjectures 4 in E the literatures, including 4 E (dxz,yz3dxy1dz21), 4 4 A1 (dxy2dxz,yz2dz21),(anti,dxy2dxz,yz2dz21dx2-y21a2u1) and A1 (anti,dxz,yz3 dxy1dz21dx2-y21a2u1). In our report, Density function theory (DFT) calculations combined with paramagnetic NMR analyses have shown the Fermi contact spin densities of 4E are more consistent with experimental data. Furthermore, through the decomposition energy composed of two fragments, containing iron porphyrin and axial cyanopyridines, the bonding interaction between iron-dxy&;#61472;and porphyrin-a1u orbitals stabilizes the intermediate spin electronic structure. Aside from the σ donating , the axial 4-CNPy also acts mainly as a π-donor instead of a π-acceptor.
author2 陳炳宇
author_facet 陳炳宇
Chiao-Han Ting
丁橋瀚
author Chiao-Han Ting
丁橋瀚
spellingShingle Chiao-Han Ting
丁橋瀚
The paramagnetic NMR study of saddledmetalloporphyrins&;#61485;1. Characterization of Saddled Nickel(III)Porphyrin Cation Radical :The NMR ExplicativeModel for Ferromagnetically CoupledMetalloporphyrin Radical.2. Saddle-shaped six-coordinate iron(III) porphyrincomplex with unusual intermediate-spinelectronic structure
author_sort Chiao-Han Ting
title The paramagnetic NMR study of saddledmetalloporphyrins&;#61485;1. Characterization of Saddled Nickel(III)Porphyrin Cation Radical :The NMR ExplicativeModel for Ferromagnetically CoupledMetalloporphyrin Radical.2. Saddle-shaped six-coordinate iron(III) porphyrincomplex with unusual intermediate-spinelectronic structure
title_short The paramagnetic NMR study of saddledmetalloporphyrins&;#61485;1. Characterization of Saddled Nickel(III)Porphyrin Cation Radical :The NMR ExplicativeModel for Ferromagnetically CoupledMetalloporphyrin Radical.2. Saddle-shaped six-coordinate iron(III) porphyrincomplex with unusual intermediate-spinelectronic structure
title_full The paramagnetic NMR study of saddledmetalloporphyrins&;#61485;1. Characterization of Saddled Nickel(III)Porphyrin Cation Radical :The NMR ExplicativeModel for Ferromagnetically CoupledMetalloporphyrin Radical.2. Saddle-shaped six-coordinate iron(III) porphyrincomplex with unusual intermediate-spinelectronic structure
title_fullStr The paramagnetic NMR study of saddledmetalloporphyrins&;#61485;1. Characterization of Saddled Nickel(III)Porphyrin Cation Radical :The NMR ExplicativeModel for Ferromagnetically CoupledMetalloporphyrin Radical.2. Saddle-shaped six-coordinate iron(III) porphyrincomplex with unusual intermediate-spinelectronic structure
title_full_unstemmed The paramagnetic NMR study of saddledmetalloporphyrins&;#61485;1. Characterization of Saddled Nickel(III)Porphyrin Cation Radical :The NMR ExplicativeModel for Ferromagnetically CoupledMetalloporphyrin Radical.2. Saddle-shaped six-coordinate iron(III) porphyrincomplex with unusual intermediate-spinelectronic structure
title_sort paramagnetic nmr study of saddledmetalloporphyrins&;#61485;1. characterization of saddled nickel(iii)porphyrin cation radical :the nmr explicativemodel for ferromagnetically coupledmetalloporphyrin radical.2. saddle-shaped six-coordinate iron(iii) porphyrincomplex with unusual intermediate-spinelectronic structure
publishDate 2014
url http://ndltd.ncl.edu.tw/handle/78982289555784286133
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